Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pentyl nitrite | HCID 10026 | — |
| Reactant | Ketene | HCID 10038 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Solvent | Heptane | HCID 8900 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | Amyl Acetate | HCID 12348 | 14% |
Reaction Steps
To the same reaction vessel as in Example 9 were charged bistriphenylphosphinedibromopalladium (0.198 g, 0.25 mmole), stannous chloride (0.095 g, 0.5 mmole), tetra-n-butylammonium chloride (0.139 g, 0.5 mmole) and n-amyl nitrite (55 ml, 368.9 mmoles), together with n-heptane (175 ml) and N-methylpyrrolidone (25 ml). Then, ketene, carbon monooxide and nitrogen were introduced to the mixture at the rate of 11.4 ml/min (0.51 mmole/min), 300 ml/min and 100 ml/min, respectively, and the reaction was effected at 90° C. for 4 hours. During the reaction, 10 ml of a solution of triphenylphosphine (0.061 g, 0.25 mmole) and stannous chloride (0.0475 g, 0.25 mmole) of N-methylpyrrolidone was added to the reaction system in 2.5 ml portions every 1 hour. The gas chromatographic analysis revealed that di-n-amyl malonate (103.9 mmoles, 84.9%) and n-amyl acetate (17.1 mmoles, 14.0%) were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04539423 |
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| Source dataset | uspto-grants-1985_09 |
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| ORD ID | ord-a860056bd5184781924258318fe60926 |
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| Source note | uspto-grants-1985_09 |
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